A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412897



Internal ID21070450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35792301..35795000hg38UCSC Ensembl
chr6:35760078..35762777hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235009
Samples
Known GenesCLPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412897
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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